Gene: ATP2A1
Official Full Name: ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 1provided by HGNC
Gene Summary: This gene encodes one of the SERCA Ca(2+)-ATPases, which are intracellular pumps located in the sarcoplasmic or endoplasmic reticula of muscle cells. This enzyme catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen, and is involved in muscular excitation and contraction. Mutations in this gene cause some autosomal recessive forms of Brody disease, characterized by increasing impairment of muscular relaxation during exercise. Alternative splicing results in three transcript variants encoding different isoforms. [provided by RefSeq, Oct 2013]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08126 | ATP2A1 Knockout cell line (HeLa) | Human | ATP2A1 | 1:3~1:6 | Negative | Online Inquiry |
KO08127 | ATP2A1 Knockout cell line (HCT 116) | Human | ATP2A1 | 1:2~1:4 | Negative | Online Inquiry |
KO08128 | ATP2A1 Knockout cell line (HEK293) | Human | ATP2A1 | 1:3~1:6 | Negative | Online Inquiry |
KO08129 | ATP2A1 Knockout cell line (A549) | Human | ATP2A1 | 1:3~1:4 | Negative | Online Inquiry |
ATP2A1 Gene Knockout Cell Lines represent a significant advancement in genetic research, providing a powerful tool for investigating the role of the ATP2A1 gene, which encodes the sarcoplasmic reticulum calcium ATPase 1 (SERCA1) protein. This protein is essential for calcium homeostasis in muscle cells and plays a critical role in muscle contraction and relaxation cycles. By employing CRISPR-Cas9 technology, these cell lines have been engineered to exhibit a complete disruption of the ATP2A1 gene, thus allowing researchers to study the downstream effects of its loss on cellular calcium signaling pathways.
The primary function of the ATP2A1 knockout is to elucidate the physiological and pathological roles of calcium ion regulation in various cell types, particularly in striated muscles. The disruption of the ATP2A1 gene can lead to profound changes in cellular physiology, providing a unique model to study muscle-related diseases, cardiac dysfunction, and potential therapeutic interventions targeting calcium dysregulation. This explores the gene's importance in development and disease states, enabling researchers to explore novel approaches in muscle regeneration, heart failure, and related conditions.
One of the standout features of ATP2A1 Gene Knockout Cell Lines is their specificity and reliability, offering a distinct advantage over traditional knockdown or overexpression techniques. By providing a stable, genetically modified line, researchers can ensure reproducibility in their experiments, a critical factor when drawing conclusions from studies involving cellular behavior. Additionally, these cell lines have been validated for their functional loss of ATP2A1 gene expression, making them a trustworthy resource for both academic and clinical researchers pursuing cutting-edge studies.
For researchers and clinicians engaged in muscle disease studies, or those exploring therapeutic targets for cardiac conditions, ATP2A1 Gene Knockout Cell Lines are invaluable. They not only simplify the complex landscape of genetic modulation but also provide a clear pathway to novel discoveries that could lead to effective treatments.
Our company prides itself on delivering high-quality biological products supported by a team of experienced scientists. With a commitment to excellence in research tools, we empower scientific inquiry with innovative products like ATP2A1 Gene Knockout Cell Lines, facilitating significant discoveries in the realms of health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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